Citrus disease cure formulation and method of treatment

ABSTRACT

An anti-bacterial composition for plants including garlic oil; cinnamon oil; yucca stem oil; oleic acid; hemp seed oil; and dimethyl sulfoxide.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application62/940,324 filed on Nov. 26, 2019 which is herein incorporated byreference in its entirety.

FIELD OF THE INVENTION

The invention relates to anti-bacterial compositions for plants andmethods of treating diseased plants.

BACKGROUND OF THE INVENTION

Citrus greening disease (also known as Huanglongbing), caused bybacterium Candidatus Liberibacter asiaticus (CLas) in the US, is aserious plant disease around the world that is posing an existentialthreat to citrus industry and has caused tremendous economic damages.Currently there is no cure or effective treatments to this disease.

The root cause of this disease is the phloem sap sucking insect Asiancitrus psyllids (Diaphorina citri) (jumping plant lice) serving as avector transmitting the bacterial pathogen. Three Gram-negative bacteriaare believed to cause greening disease in various regions: CandidatusLiberibacter asiaticus (CLas), Ca. Liberibacter africanus (CLaf), andCa. Liberibacter americanus (CLam). They are all restricted to phloemtissue in planta. Citrus greening disease in Florida, USA is caused byCLas. Ever since the insect vector Asian citrus psyllid that carried thebacterial pathogen was unknowingly introduced to the US, perhaps in the1990s, this disease has caused serious damage to Florida's citrusindustry and now is threatening other citrus growing states in the US.

In an action analogous to mosquitos, when the psyllids land on a citrusleaf and start to suck the nutritious fluid from the plant, they alsoregurgitate/introduce the bacterium CLas from their salivary tissuesinto the vascular tissue phloem of the plant. CLas proliferates insidethe phloem and clogs the transportation system for nutrients andphotosynthetic products. Over several years, the citrus tree showsstunted growth and yellowing leaves, producing greening and inediblefruits, leading to leaf and branch die out and eventual plant death,among other symptoms of the citrus greening disease. Adult psyllids liveup to several months and reproduce up to 10 generations per year. Thepsyllids feeding on the infected plants become inoculative, and tend tofly to feed on uninfected plants, thereby transmitting the bacteriafurther. Currently, this vicious cycle perpetuates to such a devastatingsituation that one should assume that in Florida every citrus tree isinfected with CLas and every psyllid likely carries CLas.

For the past decades, tremendous amounts of resources and efforts havebeen dedicated to study, treatment and management of citrus greeningdisease. Measures that have been tested include insecticide, reflectivemulch repellent, thermotherapy, fertigation and bactericides/antibioticsor viral/RNAi treatments as well as genetic engineering and transgenicapproaches. For example, starting April, 2019, citrus growers in Floridaand California start to spray antibiotics streptomycin andoxytetracycline as routing treatments for citrus greening, despite lackof convincing evidence of effectiveness.

There is therefore a need in the art for an effective citrus greeningdisease treatment.

SUMMARY OF THE INVENTION

In one aspect, there is disclosed an anti-bacterial composition forplants comprising: garlic oil; cinnamon oil; yucca stem oil; oleic acid;hemp seed oil; and dimethyl sulfoxide.

In another aspect, there is disclosed a method of treating an infectedplant comprising the steps of: forming at least one hole in the phloemof the plant; injecting a therapeutic amount of a compound comprisinggarlic oil; cinnamon oil; yucca stem oil; oleic acid; hemp seed oil; anddimethyl sulfoxide; and sealing the at least one hole.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graphical depiction of a citrus greening disease treatment;

FIG. 2A is a graph of relative CLas gene dosage for orange trees thatare treated and untreated at specified time intervals after injection;

FIG. 2B is a graph of relative CLas gene dosage for orange trees thatare treated and untreated at specified time intervals after injection;

FIG. 3A is a graph of CLas phage DNA for orange trees that are treatedand untreated at specified time intervals after injection;

FIG. 3B is a graph of CLas phage DNA for orange trees that are treatedand untreated at specified time intervals after injection;

FIG. 3C is a graph of CLas phage DNA for orange trees that are treatedand untreated at specified time intervals after injection;

FIG. 3D is a graph of CLas phage DNA for orange trees that are treatedand untreated at specified time intervals after injection;

FIG. 3E is a graph of CLas phage DNA for orange trees that are treatedand untreated at specified time intervals after injection;

FIG. 4A is a graph of transcription of CLas gene dosage for orange treesthat are treated and untreated at specified time intervals afterinjection;

FIG. 4B is a graph of transcription of CLas gene dosage for orange treesthat are treated and untreated at specified time intervals afterinjection;

FIG. 4C is a graph of transcription of CLas gene dosage for orange treesthat are treated and untreated at specified time intervals afterinjection;

FIG. 5A is an SEM images of leaf cross sections of orange plants ororange trees of the diseased orange tree #3 at magnification of ×550(A);

FIG. 5B is an SEM image of leaf cross sections of orange plants ororange trees of the diseased orange tree #3 at magnification of ×3,000;

FIG. 5C is an SEM image of leaf cross sections of orange plants ororange trees of the healthy orange tree #6 at magnification of ×800;

FIG. 5D is an SEM image of leaf cross sections of orange plants ororange trees of the healthy orange tree #6 at magnification of ×2000;

FIG. 6A is an SEM images of leaf cross sections of orange plants ofdiseased orange plant before injection (DO) at magnification of ×340;

FIG. 6B is an SEM image of leaf cross sections of orange plants ofdiseased orange plant before injection (DO) at magnification of ×850;

FIG. 6C is an SEM image of leaf cross sections of orange plants ofdiseased orange plant three weeks after injection (D3) at magnificationof ×500;

FIG. 6D is an SEM image of leaf cross sections of orange plants ofdiseased orange plant three weeks after injection (D3) at magnificationof ×700;

FIG. 6E is an SEM image of leaf cross sections of orange plants ofdiseased orange plant five weeks after injection (D5-1) at magnificationof ×400;

FIG. 6F is an SEM image of leaf cross sections of orange plants ofdiseased orange plant five weeks after injection (D5-1) at magnificationof ×850;

FIG. 6G is an SEM image of leaf cross sections of orange plants ofdiseased orange plant five weeks after injection (D5-4) at magnificationof ×440;

FIG. 6H is an SEM image of leaf cross sections of orange plants ofdiseased orange plant five weeks after injection (D5-4) at magnificationof ×800;

FIG. 7A is an NMR plots of Agent G CD₃OD (500 MHz). in the ¹H NMRprofile of Agent G;

FIG. 7B is an NMR plot of Agent G CD₃OD (500 MHz). in the ¹H-¹H COSY NMRprofile of Agent G;

FIG. 8A is a chromatogram plot of total ion chromatograms from the GC/MSof the hexane extraction of Agent G only;

FIG. 8B is a chromatogram plot of total ion chromatograms from the GC/MSof the hexane extraction of a stem without treatment;

FIG. 8C is a chromatogram plot of total ion chromatograms from the GC/MSof the hexane extraction of an 8-10 cm stem absorbing Agent G for 4 hr.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

There is disclosed an effective treatment composition herein after AgentG for citrus greening disease that was tested both in the field and inthe lab. Agent G is entirely made from plant extracts. Agent G includesthe following ingredients: garlic oil 40-50% (Example 1 45% by weight),cinnamon oil 20 to 30% (Example 1 25% by weight), Yucca stem oil 3 to 7%(Example 1 5% by weight), oleic acid 10 to 20% (Example 1 15% byweight), hemp seed oil 8 to 12% (Example 1 9.9% by weight) and dimethylsulfoxide 0.5 to 0.15 (Example 1 0.1% by weight). The weight percentagesare based on the total weight of Agent G.

In another aspect, Agent G may include the following ingredients: garlicoil (45% by weight), cinnamon oil (25% by weight), Yucca stem oil (5% byweight), oleic acid (11% by weight), hemp seed oil (9.9% by weight),dimethyl sulfoxide (0.1% by weight) and colloidal silver (4% by weight).The ranges are the same as presented above for Example 1 with the changein the amount of oleic acid with a corresponding amount of colloidalsilver. The weight percentages are based on the total weight of Agent G.

Injection of this phytolipid-suspending reagent through phloem (bark) ofthe diseased orange trees resulted in recovery in both growth and fruitproduction.

Here we report our examinations of the effects of Agent G on greeningdisease in orange plants (FIG. 1 ). Our studies show an effective andfeasible treatment that potentially could offer immediate benefit toorange growers.

Materials and Methods

Agent G

The formula design was based on the perceived antibacterial effect offour significant compounds known present in the plant extracts: allicin,saponins, flavonoids and cinnamaldehyde.

Phloemic Injection of Agent G

For this study, plants that showed yellow shots, mottled leaves withyellowing veins and several dying and brownish branches were designated“diseased”, which was then confirmed by qPCR to contain CandidatusLiberibacter asiaticus (CLas) DNA. Plants without these phenotypicsymptoms were “healthy”, from which qPCR showed undetectable orextremely low level of CLas.

Two-year-old sweet orange trees (Citrus sinensis), either healthy ordiseased, were transplanted from an orange grove to a growth room andgrown at 25° C. under 8 hr of darkness and 16 hr of cool white light of250 μmol photons m²/s. To inject Agent G, four 5-mm holes were drilledby a 2-mm drill bit at the base of the tree (7 to 8 cm incircumference). Approximately 0.3 mL of Agent G was injected into eachhole with a syringe and a 18G1 needle. The holes were sealed withPruning Seal (Spectracide).

Three to 8-year-old orange trees grown in a plot of an orange grove inSarasota, Fla., showed symptoms of greening disease. Injections weredone to five orange trees, whereas other trees were left untreated.

DNA and RNA Extraction and qPCR Analysis

At least three leaves including petiole were collected from separatepositions on each of healthy and diseased trees grown both in the growthroom and in the Sarasota grove. Leaflets of each trifoliolate leaf werecut into two halves along the middle vein and used for extraction of DNAand RNA and for scanning electron microscopy. Leaves were ground inliquid N2 to fine powders with mortars and pestles. Genomic DNA wasextracted using GenCatch Plant Genomic DNA Miniprep kit (Epoch LifeScience, USA) with RNase treatment. RNA was extracted using Total RNAMini kit (plant) (Geneaid/FroggaBio, USA) with DNase treatment.First-strand cDNA was made using SuperScript IV reverse transcriptase(Invitrogen, USA) and oligo dT and random primers according tomanufacturer's instruction.

Quantitative real-time PCR (qPCR) using SYBR Green (Life Technologies,USA) was carried out to examine the presence of CLas DNA. Two orangeplant genes, elongation factor 1-α (EF) and cytochrome oxidase, wereused as references for ΔCt normalization. Results with EF are reportedhere. To detect CLas bacteria, four CLas genes were tested: prophagerepeat (PR), elongation factor Ts, 16S rDNA and ribosomal protein L12P,whose primers were designed based on known reports. To detect CLasprophage, five phage genes were tested: peroxidase, glutathioneperoxidase, tail fiber, holin and endolysin.

qPCR was also performed to measure the relative transcription levels ofseveral CLas and prophage genes, using the constitutively expressedorange plant cytochrome oxidase gene used as the internal reference.

Scanning Electron Microscopic Observation

Orange leaves including petioles were fixed with 2% glutaraldehyde at24° C. overnight, followed by dehydration with a series of ethanolsolutions from 30% to 100%. Then the dehydrated leaves were ground andfractured in liquid nitrogen, and immediately immerged in 100% ethanol.For scanning electron microscopy imaging, samples were critical-pointdried, mounted and gold-coated for viewing with Leica EM CPD300 systemaccording to manufacturer's instructions. At least three leaves fromeach plant, most coupled with qPCR assays, were processed and viewed.

NMR and GC/MS Analysis of Agent G

The 1H and 1H-1H COSY NMR spectra of Agent G were recorded in CD3OD on aVarian UNITY INOVA 500 MHz spectrometer. Chemical shifts (δ) werereferenced internally to the residual solvent peak (CD3OD: 1H, δH 3.31ppm).

The Agent G cocktail was also subjected to Gas Chromatography-MassSpectroscopy (GC/MS) analysis. The analysis was conducted using aPerkin-Elmer AutoSystem XL gas chromatograph, paired with a Perkin-ElmerTurboMass Gold mass spectrometer. The GC was equipped with an Elite-5capillary column with helium as carrier gas and a flow rate of 1 μL/minwhich was used for separation of compounds. The instrument was set to aninitial temperature of 70° C., and maintained at this temperature for 5min. The oven temperature was raised up to 270° C., at the rate of 5°C./min, and maintained for 9 min. Injection port temperature was ensuredas 250° C. and Helium flow rate as one ml/min. The ionization voltagewas 70 eV. The MS was used to further analyze compounds and was operatedin EI mode. Mass spectral scan range was set at 100-500 (m/z). Theindividual peaks were identified by comparing their mass spectra withthe National Institute Standard and Technology mass spectral database(NIST) and then the compounds of MS matching similarity ≥90% wereselected as results.

Phloem Loading Rate Measurements by GC/MS

Detached branches of the tree were placed in a solution of Agent G underwhite light of 250 μmol photons m²/s at 25° C. for periods of 4 and 8hrs. Then the stems were cut into segments of 2 cm in length starting at10 cm and stored at −80° C. The samples were chopped into pieces of ˜0.2cm, and then immediately submerged into 1 mL of hexanes. The sampleswere then placed into an ultrasonic bath (25° C.) for 1 hr and extractedovernight (24 hr) prior to GC/MS analysis. The sample solutions wereinjected into the GC/MS with a volume of 5 μL, and analyzed by GC/MS asdescribed above.

Orange Fruit Yield Measurements

Five to eight-year-old orange trees with obvious heavy symptoms ofgreening disease and significant die back did not produce any ediblefruits during 2014-2015 growth season were injected in 2015 with theAgent G. These trees were cared for as normally as for other trees.During 2015-2016 season, plant growth was monitored visually and withphotographs. Orange fruits were harvested and weighed.

Statistical Analysis

For qPCR analysis, three replicates for each assay were performed. Thedifferences doe gene dosages or gene expression levels were tested usingone way ANOVA coupled with Games-Howell (equal variance not assumed) andthe Least Significant Difference (LSD) methods (equal variance assumed)with the corresponding patterns of experimental data. Statisticalanalysis was performed using SPSS software (ver. 16.0). The significantlevel was set at P<0.05.

Results

Detection of CLas bacteria

We employed qPCR to detect the presence of CLas bacteria in leaves, asqPCR may detect as little as one copy of bacterial DNA in the sample. Tomitigate the drawback of uneven CLas distribution throughout the plant,we sampled 3 to 5 leaves from each tree. We tested primers for fourpreviously reported CLas genes all of which worked well and the prophagerepeat seemed more sensitive. Here we show the results with the prophagerepeat primers.

Eight grove-grown orange trees were tested. The previously diseasedtrees recovered to a healthy phenotype after injection. qPCR analysisshowed that those treated plants (trees #1, #2, #4 and #5) haddiminishing levels of CLas, decreasing as much as 3,000 fold, ascompared to the diseased tree #3 but they still had detectable CLas,whereas CLas was not detected in the non-injected one-year-old healthytrees #6, #7 and #8 (FIG. 2A).

Likewise, in the growth chamber, the symptomatically diseased plant hada high level of CLas DNA (FIG. 2B). After injection of Agent G, thephenotype of the diseased plant appears gradually improved with greenerleaves. At 3 weeks and 5 weeks after injection, CLas DNA levels dropped1,100˜3,100 folds to very low, although detectable, levels in both newlyemerged leaves and older leaves that existed prior to injection (FIG.2B). These qPCR results indicate that one-time injection of Agent Ggreatly reduced the CLas bacterial load in the leaves, although totalCLas elimination was not achieved.

Detection of CLas Prophages and Gene Expression

All pathogenic CLas strains are known to have prophages. Due to thepresence of CLas bacteria, CLas phage lytic genes (holing, glutathioneperoxidase, tail fiber, endolysin and peroxidase) were all detected inthe diseased plant (FIG. 3 ). Three or 5 weeks after injection, therelative dosages of these phage genes greatly decreased (FIG. 3A-C), orin some cases undetectable (FIG. 3D, E). This observation is consistentwith the detection of CLas bacterial DNA (FIG. 2 ), confirming theco-existence of prophages with CLas bacteria in the diseased plants.

Interestingly, transcription of prophage genes holin and glutathioneperoxidase was apparently elevated after Agent G injection as comparedto before injection (FIG. 4A, B). There was also marked expression ofphage tail fiber gene after injection (FIG. 4C). This becomes morestriking when considering much lower gene dosages after injection (FIG.3A, B, C). No transcription was detected for prophage genes endolysinand peroxidase.

Scanning Electron Microscopy Examination

Leaves of field-grown trees #3 (diseased) and #6 (healthy) were examinedby scanning electron microscopy (SEM). Consistent with the qPCR results(FIG. 2 ), SEM revealed bacterial colonization inside the phloem fibercells of the infected tree (FIG. 5A, B). Rod-shaped bacteria were foundclumped together and clogged the phloem fiber cells. By contrast, theleaves of the healthy tree, where CLas was not detected by qPCR (FIG.2A), showed the phloem tissue clear of deposits, indicating a clean,smooth vascular system (FIG. 5C, D).

Similarly, SEM exhibited significant clogs in the phloem tissue of thelab-grown diseased plant before injection (DO; FIG. 6A, B), which wasfound to have a high level of CLas bacterial DNA (FIG. 2B). Three tofive weeks after injection, bacterial colonies in the phloem fibertissues diminished markedly although not completely disappeared (FIG. 6Cto H). These results further indicate that injection of Agent G promotesclearance of CLas bacterial clogs in phloem tissue.

Chemical Composition Analysis of Agent G

The chemical composition of Agent G was evaluated by NMR and GC/MSanalysis. The 1H NMR spectrum (FIG. 7A) of Agent G revealed a complexmixture of compounds. The major components included a series ofcompounds containing proton signals in the olefinic region between 5-6ppm and doublet signals between 3-4 ppm, consistent with thioallyllicprotons, and indicated the presence of allyl polysulfides as observed inthe 1H NMR spectrum of garlic oil. In addition, the 1HMR spectrumrevealed the proton signals of aromatic aldehydes at δ 9.67 and 9.62 ppmand a series of signals in the aromatic and olefinic region of thespectrum consistent with phenylpropanoids. This was confirmed with aseries of cross peaks between these signals in the 1H-1H COSY spectrum(FIG. 7B) and allowed the identification of (E)-cinnamaldehyde ando-hydroxycinnamaldehyde, as previously observed in 1H NMR spectrum ofcinnamon oil. The NMR data also revealed the presence of other signalsassociated with fatty acids, carbohydrates and steroids.

Furthermore, the GC/MS of the hexane extract of Agent G showed thepresence of a large number of compounds with six major compounds beingidentified based on the NIST library search (Table 1; FIG. 8A). Thesecompounds were mostly allyl polysulfides with the major compounds beingdiallyl disulfide and diallyl trisulfide from garlic oil andcinnamaldehyde from cinnamon oil, as previously identified by NMR. TheGC/MS also revealed the presence of an unknown compound (compound Y)with retention time of 9.59 minutes and a molecular ion at m/z 147 (FIG.8A) that could not be identified.

TABLE 1 Major compounds identified in Agent G from GC/MS and migrationrates. Mass Migration CAS Molecular Retention Spec Distance Rate NumberCompound Name number Formula Time (m/z) Traveled (cm/hr) 1 2,5-Dimethyl-27464-82-0 C₄H₆N₂S 1.71 114 14 cm 1.75 1,3,4-thiadiazole 2 Diallyldisulfide 2179-57-9 C₆H₁₀S₂ 4.10 146 24 cm 3.0 3 Cinnamaldehyde 104-55-2C₉H₈O 6.12 132 12 cm 1.50 4 Diallyl Trisulfide 2050-87-5 C₉H₁₀S₃ 6.32178 26 cm 3.25 5 Allyl 41820-22-8 C₆H₁₀OS 8.02 146 24 cm 3.0Thiopropionate 6 Unidentified — — 9.59 147 18 cm 2.25 Compound Y

Phloemic Migration Rate

To assess the phloemic migration of the injected reagent, stem segments(FIG. 8B, C) were extracted with hexane and analyzed by GC/MS toidentify common volatile components. Only one compound, themonoterpenoid citral or lemonal, with a retention time of 6.08 min.overlapped with cinnamaldehyde with a retention time of 6.12 min.However, as the mass and the fragmentation pattern was different forthat of citral, the migration rate of cinnamaldehyde in the stem couldstill be determined. GC/MS analysis of the stem sections withouttreatment served as base profile (FIG. 8B). After absorption in Agent Gfor 4 hours the 8-10 cm stem segment revealed only the major components,diallyl disulfide and diallyl trisulfide (FIG. 8C) but not in the 18-20cm or the 28-30 cm sections of the stem. After 8 hours soaking all sixmajor components of Agent G were detected in sections of the stem atvarious distances (Table 1). Migration rates were estimated to be in arange of 1.5-3.25 cm/hr, which confirm the ability of Agent G to betransported through the phloem (bark).

Field Test

Formulation and testing of plant derived antibacterials foreffectiveness against the CLas bacterium began in 2014 with infectedorange trees in Sarasota, Fla. It was determined that the efficacy ofinjections into the phloem of these trees was enhanced by using acocktail of multiple plant extracts. Five to eight-year-old trees withobvious heavy infection and significant die back were eventuallyinjected in 2015 with the cocktail. Those injected trees recoveredphenotypically. Trees with no yield during the 2014-15 season recoveredsufficiently to produce more than 45 kg of healthy orange fruits perinjected tree in the 2016-2017 season.

Discussion

Our studies found that injection of the plant extract cocktail Agent Gthrough phloem is effective in treating green disease in orange plants.This conclusion is based on following observations: first, afterinjection, the levels of CLas, the causing pathogen for citrus greeningdisease, decreased thousands fold in the leaves, as indicated by qPCRusing CLas specific primers (FIG. 2 ). Second, after injection, thelevels of CLas prophage DNA also decreased significantly, yet someprophage gene expression was elevated (FIGS. 3 and 4 ). Third, afterinjection, the bacterial clogs in phloem tissue were noticeablylessened, in contrast with heavily clogged phloem fiber cells beforeinjection, as revealed by scanning electron microscopy (FIGS. 5 and 6 ).Finally, although empirically, after injection, the diseased plantsrecovered in growth phenotypically and fruit production recovered, ascompared to the untreated non-producing diseased trees.

Our studies clearly show strong inhibitory effect of Agent G on CLas inplanta. Various unique compounds of allyl polysulfides andcinnamaldehydes were found in Agent G and the treated stem samples(Table 1; FIGS. 7 and 8 ) but not in untreated plants. These compoundstraveled through the phloem tissues (FIG. 8 ). Although the activeingredients in Agent G are not precisely known, while not wishing to bebound by theory since allicin, saponins, flavonoids and cinnamaldehydepresent in Agent G exhibit antibacterial effects across a broad range ofbacteria their direct contact with CLas bacteria through phloem tissueswould cause immediate bactericide. Combination of these compounds alongwith many other unknown plant metabolites may also synergisticallyenhance the antibacterial effectiveness by Agent G.

Presence of CLas prophages in the infected plants is expected becauseall known CLas strains possess the prophages. However, it is interestingto observe elevated expression of CLas phage lytic genes holin andglutathione peroxidase, to a lesser extent tail fiber, after phloemicinjection. It has been found that expression of CLas prophage genesholin, tail fiber and peroxidases was much higher in infected non-hostplant periwinkle than in infected host citrus plants, suggesting anegative association between prophage activity and CLaspathogenicity/infectivity. Particularly, holins are transmembraneproteins that are produced by prophages during late gene expression.Aggregation of holin proteins triggers disruption of bacterial innermembrane, leading to degradation of cell walls and bacterial cell death.It is possible that ingredients of Agent G activated some of the phagelytic genes such as holins and thus promoted the destruction of CLasbacteria. Phage activation leading to bacterial “suicide” can be apowerful means to suppress CLas pathogenicity and cure greening disease.

Due to current dire lack of effective methods to control serious plantdiseases, crop growers increasingly turn to antibiotics for quicktreatments, such as spraying citrus plants to fight greening disease.This practice of large-scale antibiotic spraying has the potential offacilitating antimicrobial resistance in the environment. Thus, the factthat Agent G is made entirely from plant extracts, without medicalantibiotics or toxic, polluting chemicals, makes it environmentallynon-impacted and acceptable to both growers and consumers.

There is no reason to expect Agent G acts specifically on bacterium CLasor orange plants. Agent G via phloemic injection should have similarantibacterial effect on other bacterial pathogens and in other plants.Therefore, this regimen could be useful for disease control andmanagement for other crops. Also due to the complex chemical nature ofplant extracts in Agent G and possible synergistic effect of theseingredients, application of Agent G should be less likely for bacteriato develop resistance quickly, as opposed to use of formularyantibiotics.

The invention claimed is:
 1. An anti-bacterial composition for plantscomprising: garlic oil; cinnamon oil; yucca stem oil; oleic acid ispresent in an amount of from 10 to 20% by weight; hemp seed oil ispresent in an amount of from 8 to 12% by weight; and dimethyl sulfoxideis present in an amount of from 0.5 to 0.15% by weight, the weightsbased on a total weight of the composition.
 2. The anti-bacterialcomposition for plants of claim 1 wherein garlic oil is present in anamount of from 40 to 50% by weight; cinnamon oil is present in an amountof from 20 to 30% by weight; yucca stem oil is present in an amount offrom 3 to 7% by weight; the weights based on a total weight of thecomposition.
 3. The anti-bacterial composition for plants of claim 1wherein garlic oil is present in an amount of 45% by weight; cinnamonoil is present in an amount of 25% by weight; yucca stem oil is presentin an amount of 5% by weight; oleic acid is present in an amount of 15%by weight; hemp seed oil is present in an amount of 9.9% by weight; anddimethyl sulfoxide is present in an amount of 0.1% by weight, theweights based on a total weight of the composition.
 4. Theanti-bacterial composition for plants of claim 1 wherein the compositionincludes allicin, saponins, flavonoids and cinnamaldehyde.
 5. Theanti-bacterial composition for plants of claim 4 wherein the compositionincludes 2,5-Dimethyl-1,3,4-thiadiazole, Diallyl disulfide,Cinnamaldehyde, Diallyl Trisulfide, Allyl Thiopropionate and compound Yhaving a molecular ion at m/z
 147. 6. The anti-bacterial composition forplants of claim 1 further including colloidal silver.
 7. A method oftreating an infected plant comprising the steps of: forming at least onehole in the phloem of the plant; injecting a therapeutic amount of acomposition comprising garlic oil; cinnamon oil; yucca stem oil; oleicacid is present in an amount of from 10 to 20% by weight; hemp seed oilis present in an amount of from 8 to 12% by weight; and dimethylsulfoxide is present in an amount of from 0.5 to 0.15% by weight, theweights based on a total weight of the composition; sealing the at leastone hole.
 8. The method of claim 7 wherein the plant is infected withCandidatus Liberibacter asiaticus (CLas).
 9. The method of claim 8wherein 3 to 5 weeks after injection CLas DNA levels dropped 1,100 to3,100 fold.
 10. The method of claim 8 wherein 3 to 5 weeks afterinjection CLas phage lytic genes of holing, glutathione peroxidase, tailfiber, endolysin and peroxidase decreased.
 11. The method of claim 8wherein 3 to 5 weeks after injection bacterial colonies in the phloemdiminished.
 12. The method of claim 7 wherein a phloemic migration ofthe composition is from 1.5-3.25 cm/hr.
 13. The method of claim 8wherein the composition activates phage lytic genes and promotesdestruction of CLas bacteria.
 14. The method of claim 7 wherein garlicoil is present in an amount of from 40 to 50% by weight; cinnamon oil ispresent in an amount of from 20 to 30% by weight; yucca stem oil ispresent in an amount of from 3 to 7% by weight; the weights based on atotal weight of the composition.
 15. The method of claim 7 whereingarlic oil is present in an amount of 45% by weight; cinnamon oil ispresent in an amount of 25% by weight; yucca stem oil is present in anamount of 5% by weight; oleic acid is present in an amount of 15% byweight; hemp seed oil is present in an amount of 9.9% by weight; anddimethyl sulfoxide is present in an amount of 0.1% by weight, theweights based on a total weight of the composition.
 16. The method ofclaim 7 wherein the composition includes allicin, saponins, flavonoidsand cinnamaldehyde.
 17. The method of claim 16 wherein the compositionincludes 2,5-Dimethyl-1,3,4-thiadiazole, Diallyl disulfide,Cinnamaldehyde, Diallyl Trisulfide, Allyl Thiopropionate and compound Yhaving a molecular ion at m/z
 147. 18. The method of claim 7 furtherincluding colloidal silver.
 19. An anti-bacterial composition for plantscomprising: garlic oil is present in an amount of 45% by weight;cinnamon oil is present in an amount of 25% by weight; yucca stem oil ispresent in an amount of 5% by weight; oleic acid is present in an amountof 15% by weight; hemp seed oil is present in an amount of 9.9% byweight; and dimethyl sulfoxide is present in an amount of 0.1% byweight, the weights based on a total weight of the composition.